Editable Word and Excel systems that help testing-lab quality managers plan audits, trace evidence, close findings, and stay ready for assessment.
Start with a focused readiness review, run a complete internal audit, or get both systems together. Every file is ready to download and edit.
A complete, white-label internal audit system for testing labs. Plan, audit, track findings, and report to management.
Find out exactly how ready your lab is for ISO/IEC 17025 accreditation. Review 77 requirements across clauses 4–8, score readiness, and build an action plan.
The 10 Most Common ISO/IEC 17025 Internal Audit Findings — each paired with a practical fix your lab can use.
The Internal Audit Kit and Gap Analysis together: diagnose where you stand, then run the audit with one connected toolkit.
Eight white-label template packs covering the records assessors ask for most — from document control to analytical QC. Buy individually, or take the whole library.
Procedure, control matrix, master document list, change requests, and distribution records. Clauses 8.2–8.3.
Master list, maintenance and calibration logs, daily balance checks, and instrument use logbooks. Clause 6.4.
Training records, competency assessments, training matrix, and impartiality records. Clauses 6.2 and 4.
CAPA forms and tracker, root cause checklist, risk register, and change impact assessment. Clauses 8.5, 8.7.
Approved supplier list, evaluation criteria, and confidentiality agreements. Clause 6.6.
Chain of custody, collection forms, report amendments, and disposal logs. Clauses 7.4, 7.8.8.
Seven ready-to-print logbooks: environmental, solution prep, reagents, housekeeping, visitors, secure access. Clause 6.3.
Batch QC logs, run worksheets, reference standard log, plus incident and feedback forms. Clause 7.7.
All 8 packs — 39 white-label templates covering every record an assessor asks for, from document control to analytical QC.
These are not generic ISO 9001 documents with laboratory terms added later. The structure is designed for testing-lab evidence, records, findings, and follow-through.
Focused on the systems, records, and technical evidence used in testing laboratories.
Organized around how assessors trace requirements to procedures, records, and objective evidence.
Word and Excel files are ready for your terminology, responsibilities, scope, and workflow.
No vendor branding. Download immediately, add your lab identity, and start working.
Questions about fit, editing, and what the kits do—and do not—include.
No. You’ll need to purchase your own authorized copy of ISO/IEC 17025 from ISO or another approved standards provider.
No. No kit can guarantee accreditation. The documents help you organize and perform the work; your laboratory remains responsible for implementation, evidence, technical competence, and meeting your accreditation body’s requirements.
Yes. The Word and Excel files are fully editable so you can add your lab name, roles, scope, methods, terminology, and existing process details.
This is the testing-laboratory edition. A calibration-laboratory edition is planned.
See ten recurring audit issues and the practical fix for each one.